Journal of
Medicinal Plants Research

  • Abbreviation: J. Med. Plants Res.
  • Language: English
  • ISSN: 1996-0875
  • DOI: 10.5897/JMPR
  • Start Year: 2007
  • Published Articles: 3834

Full Length Research Paper

Function-structural study of anti-LDL-oxidation effects of flavonoid phytochemicals

Yiwen Yao1#, Shuqing Liu2#, Chunmei Guo3, Chunyan Zhang3, Dachang Wu3, Yixin Ren2, Hong-Shan Yu4, Ming-Zhong Sun3 and Hailong Chen5*
1Department of Otolaryngology, the First affiliated Hospital of Dalian Medical University, Dalian 116011, China. 2Department of Biochemistry, Dalian Medical University, Dalian 116044, China. 3Department of Biotechnology, Dalian Medical University, Dalian 116044, China. 4School of Bioengineering, Dalian Polytechnic University, Dalian 116034, China. 5Department of Surgery, the First Affiliated Hospital of Dalian Medical University, Dalian 116011, China
Email: [email protected]

  •  Accepted: 09 March 2012
  •  Published: 25 December 2012

Abstract

As a large group of polyphenolic phytochemicals with excellent anti-oxidation properties, the dietary flavonoid intakes have been shown to be negatively correlated with the incidence of coronary artery disease. Flavonoid compounds potentially inhibit the oxidation of low-density lipoprotein (Ox-LDL) that triggers the generation of a series of oxidation byproducts playing important roles in atherosclerosis development. The diverse inhibitory effects of different flavonoid phytochemicals on Ox-LDL might be closely associated with their intrinsic structures. In current work, we investigated the effects of eight flavonoid phytochemicals in high purity (>95%) with similar core structure on the susceptibility of LDL to Cu2+-induced oxidative modification. The results indicated that quercetin, rutin, isoquercitrin, hesperetin, naringenin, hesperidin, naringin and icariin could reduce the Cu2+-induced-LDL oxidation by59.56±7.03, 46.53±2.09, 40.52±4.65, 22.67±1.68, 20.87±2.43, 12.34±2.09, 10.87±1.68 and 3.53±3.20%, respectively. The function-structure relation study indicated that: (1) for structure similar flavonoids, the flavonoids with more free phenolic hydroxyl groups showed relative higher anti-Ox-LDL activities; (2) the free 3-OH in the C ring of flavones was important for the anti-Ox-LDL activities of flavonol (quercetin) and flavones (rutin and isoquercitrin) as their activities were decreased by ~22 and ~32% following the b-Glc and b-Glc-a-Rha modifications of 3-OH; (3) the 7-OH of A ring was important for anti-Ox-LDL capacities of flavanone compounds. The substitution of b-Glc-a-Rha with the hydrogen of 7-OH made the anti-Ox-LDL abilities for hesperidin and naringin reduced by 45.6 and 47.9%; (4) function and structure comparison also indicated that the C ring C2-C3 double bond and the 4’-OH might benefit the protection of Cu2+-induced LDL oxidation by flavonoids. Taken together, the anti-Ox-LDL activities of flavonoids were closely associated with their intrinsic structures/conformations. This study might provide clues to estimate/evaluate the contribution impacts of different functional groups of flavonoids on anti-LDL oxidation, which might also help in selecting effective and favorable dietary flavonoid drugs in the prevention and treatment of coronary artery disease and similar diseases.

 

Key words: Flavonoid phytochemicals, low-density lipoprotein (LDL) oxidation, antioxidant, function, structure.